Cost-effectiveness of second-line therapies in adults with chronic immune thrombocytopenia.


Journal

American journal of hematology
ISSN: 1096-8652
Titre abrégé: Am J Hematol
Pays: United States
ID NLM: 7610369

Informations de publication

Date de publication:
01 2023
Historique:
received: 04 02 2022
accepted: 07 02 2022
pubmed: 12 2 2022
medline: 23 12 2022
entrez: 11 2 2022
Statut: ppublish

Résumé

Major options for second-line therapy in adults with chronic immune thrombocytopenia (ITP) include splenectomy, rituximab, and thrombopoietin receptor agonists (TRAs). The American Society of Hematology guidelines recommend rituximab over splenectomy, TRAs over rituximab, and splenectomy or TRAs while noting a lack of evidence on the cost-effectiveness of these therapies. Using prospective, observational, and meta-analytic data, we performed the first cost-effectiveness analysis of second-line therapies in chronic ITP, from the perspective of the U.S. health system. Over a 20-year time-horizon, our six-strategy Markov model shows that a strategy incorporating early splenectomy, an approach at odds with current guidelines and clinical practice, is the cost-effective strategy. All four strategies utilizing TRAs in the first or second position cost over $1 million per quality-adjusted life-year, as compared to strategies involving early use of splenectomy and rituximab. In a probabilistic sensitivity analysis, early use of splenectomy and rituximab in either order was favored in 100% of 10 000 iterations. The annual cost of TRAs would have to decrease over 80% to begin to become cost-effective in any early TRA strategy. Our data indicate that effectiveness of early TRA and late TRA strategies is similar with the cost significantly greater with early TRA strategies. Contrary to current practice trends and guidelines, early use of splenectomy and rituximab, rather than TRAs, constitutes cost-effective treatment in adults with chronic ITP.

Identifiants

pubmed: 35147241
doi: 10.1002/ajh.26497
pmc: PMC9365880
mid: NIHMS1820204
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Thrombopoietin 9014-42-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122-130

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007517
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Informations de copyright

© 2022 The Authors. American Journal of Hematology published by Wiley Periodicals LLC.

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Auteurs

George Goshua (G)

Section of Hematology, Yale University School of Medicine, New Haven, Connecticut, USA.
Department of Health Policy and Management, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Pranay Sinha (P)

Department of Health Policy and Management, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Section of Infectious Diseases, Boston Medical Center, Boston, Massachusetts, USA.

Natalia Kunst (N)

Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Healthcare Institute, Boston, Massachusetts, USA.

Lauren Pischel (L)

Section of Infectious Diseases, Yale University School of Medicine, New Haven, Connecticut, USA.
Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, USA.

Alfred Ian Lee (AI)

Section of Hematology, Yale University School of Medicine, New Haven, Connecticut, USA.

Adam Cuker (A)

Department of Medicine and Department of Pathology & Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

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Classifications MeSH